Lead safety surveillance and risk-benefit activities for assigned products.
Define strategy for signal detection and oversight of safety signals.
Prepare and approve safety deliverables (PSURs/DSURs/RMPs).
Translate safety data into actionable recommendations for decisions.
Represent Safety Science in MDT and integrate safety into development decisions.
Collaborate cross-functionally to ensure lifecycle safety decisions.

🎯 Requirements

MD, PharmD, PhD or Master’s in Life Sciences/Public Health.
Solid experience in pharmacovigilance and safety science.
Strong knowledge of global PV regulations (GVP, ICH E2E).
Proficiency to analyze and synthesize medical safety data.
Proficiency in Excel, SQL, and data viz tools (Power BI, Spotfire).
Experience leading cross-functional global product safety teams and safety strategy.

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